A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666584



Internal ID15403236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82233648..82292466hg38UCSC Ensembl
Innerchr10:83993404..84052222hg19UCSC Ensembl
Innerchr10:83983384..84042202hg18UCSC Ensembl
Innerchr10:83983384..84042202hg17UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3858819
hg1958819
hg1858819
hg1758819
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516167
Supporting Variants
Samples
Known GenesNRG3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv666584
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer